348074
2-氯-4-氟苯甲醛
97%
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关于此项目
线性分子式:
ClC6H3(F)CHO
化学文摘社编号:
分子量:
158.56
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
Quality Level
assay
97%
form
solid
bp
118-120 °C/50 mmHg (lit.)
mp
60-63 °C (lit.)
functional group
aldehyde, chloro, fluoro
SMILES string
Fc1ccc(C=O)c(Cl)c1
InChI
1S/C7H4ClFO/c8-7-3-6(9)2-1-5(7)4-10/h1-4H
InChI key
KMQWNQKESAHDKD-UHFFFAOYSA-N
General description
2-Chloro-4-fluorobenzaldehyde is a halogen substituted benzaldehyde.
Application
2-Chloro-4-fluorobenzaldehyde may be used in the synthesis of substituted α-cyanocinnamic acid, via Knoevenagel condensation reaction. It may be used in the synthesis of 2-(2-benzimidazolyl)-3-(2-chloro-4-fluorophenyl)acrylonitrile.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
商品
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
Biological activity and DNA binding studies of 2-substituted benzimidazo [1, 2-a] quinolines bearing different amino side chains.
Perin N, et al.
MedChemComm, 4(12), 1537-1550 (2013)
Thorsten W Jaskolla et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(34), 12200-12205 (2008-08-30)
Matrix-assisted laser desorption ionization (MALDI) has become an enabling technology for the fields of protein mass spectrometry (MS) and proteomics. Despite its widespread use, for example, in protein identification via peptide mass fingerprinting, a comprehensive model for the generation of
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 348074-1G | 04061826072349 |
| 348074-5G | 04061832491745 |